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Refinado por: Base de dados/Biblioteca: EBSCO_MEDLINE Complete（医学期刊全文数据库） remover assunto: Genetics remover
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1
Abundant quantitative trait loci exist for DNA methylation and gene expression in human brain
Abundant quantitative trait loci exist for DNA methylation and gene expression in human brain
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Abundant quantitative trait loci exist for DNA methylation and gene expression in human brain

Gibbs, J Raphael ; van der Brug, Marcel P ; Hernandez, Dena G ; Traynor, Bryan J ; Nalls, Michael A ; Lai, Shiao-Lin ; Arepalli, Sampath ; Dillman, Allissa ; Rafferty, Ian P ; Troncoso, Juan ; Johnson, Robert ; Zielke, H Ronald ; Ferrucci, Luigi ; Longo, Dan L ; Cookson, Mark R ; Singleton, Andrew B Flint, Jonathan

PLoS genetics, 2010-05, Vol.6 (5), p.e1000952-e1000952 [Periódico revisado por pares]

United States: Public Library of Science

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2
High-resolution inference of genetic relationships among Jewish populations
High-resolution inference of genetic relationships among Jewish populations
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High-resolution inference of genetic relationships among Jewish populations

Kopelman, Naama M ; Stone, Lewi ; Hernandez, Dena G ; Gefel, Dov ; Singleton, Andrew B ; Heyer, Evelyne ; Feldman, Marcus W ; Hillel, Jossi ; Rosenberg, Noah A

European journal of human genetics : EJHG, 2020-06, Vol.28 (6), p.804-814 [Periódico revisado por pares]

England: Nature Publishing Group

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3
Genome wide assessment of young onset Parkinson's disease from Finland
Genome wide assessment of young onset Parkinson's disease from Finland
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Genome wide assessment of young onset Parkinson's disease from Finland

Hernandez, Dena G ; Nalls, Michael A ; Ylikotila, Pauli ; Keller, Margaux ; Hardy, John A ; Majamaa, Kari ; Singleton, Andrew B Toft, Mathias

PloS one, 2012-07, Vol.7 (7), p.e41859-e41859 [Periódico revisado por pares]

United States: Public Library of Science

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4
Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation
Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation
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Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation

Wood, Andrew R ; Perry, John R B ; Tanaka, Toshiko ; Hernandez, Dena G ; Zheng, Hou-Feng ; Melzer, David ; Gibbs, J Raphael ; Nalls, Michael A ; Weedon, Michael N ; Spector, Tim D ; Richards, J Brent ; Bandinelli, Stefania ; Ferrucci, Luigi ; Singleton, Andrew B ; Frayling, Timothy M Arking, Dan E.

PloS one, 2013-05, Vol.8 (5), p.e64343-e64343 [Periódico revisado por pares]

United States: Public Library of Science

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5
Resolving the polymorphism-in-probe problem is critical for correct interpretation of expression QTL studies
Resolving the polymorphism-in-probe problem is critical for correct interpretation of expression QTL studies
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Resolving the polymorphism-in-probe problem is critical for correct interpretation of expression QTL studies

Ramasamy, Adaikalavan ; Trabzuni, Daniah ; Gibbs, J Raphael ; Dillman, Allissa ; Hernandez, Dena G ; Arepalli, Sampath ; Walker, Robert ; Smith, Colin ; Ilori, Gigaloluwa Peter ; Shabalin, Andrey A ; Li, Yun ; Singleton, Andrew B ; Cookson, Mark R ; Hardy, John ; Ryten, Mina ; Weale, Michael E

Nucleic acids research, 2013-04, Vol.41 (7), p.e88-e88 [Periódico revisado por pares]

England: Oxford University Press

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6
Genome-wide meta-analysis for serum calcium identifies significantly associated SNPs near the calcium-sensing receptor (CASR) gene
Genome-wide meta-analysis for serum calcium identifies significantly associated SNPs near the calcium-sensing receptor (CASR) gene
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Genome-wide meta-analysis for serum calcium identifies significantly associated SNPs near the calcium-sensing receptor (CASR) gene

Kapur, Karen ; Johnson, Toby ; Beckmann, Noam D ; Sehmi, Joban ; Tanaka, Toshiko ; Kutalik, Zoltán ; Styrkarsdottir, Unnur ; Zhang, Weihua ; Marek, Diana ; Gudbjartsson, Daniel F ; Milaneschi, Yuri ; Holm, Hilma ; Diiorio, Angelo ; Waterworth, Dawn ; Li, Yun ; Singleton, Andrew B ; Bjornsdottir, Unnur S ; Sigurdsson, Gunnar ; Hernandez, Dena G ; Desilva, Ranil ; Elliott, Paul ; Eyjolfsson, Gudmundur I ; Guralnik, Jack M ; Scott, James ; Thorsteinsdottir, Unnur ; Bandinelli, Stefania ; Chambers, John ; Stefansson, Kari ; Waeber, Gérard ; Ferrucci, Luigi ; Kooner, Jaspal S ; Mooser, Vincent ; Vollenweider, Peter ; Beckmann, Jacques S ; Bochud, Murielle ; Bergmann, Sven Abecasis, Gonçalo R.

PLoS genetics, 2010-07, Vol.6 (7), p.e1001035-e1001035 [Periódico revisado por pares]

United States: Public Library of Science

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7
Genomic risk profiling of ischemic stroke: results of an international genome-wide association meta-analysis
Genomic risk profiling of ischemic stroke: results of an international genome-wide association meta-analysis
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Genomic risk profiling of ischemic stroke: results of an international genome-wide association meta-analysis

Meschia, James F ; Singleton, Andrew ; Nalls, Michael A ; Rich, Stephen S ; Sharma, Pankaj ; Ferrucci, Luigi ; Matarin, Mar ; Hernandez, Dena G ; Pearce, Kerra ; Brott, Thomas G ; Brown, Jr, Robert D ; Hardy, John ; Worrall, Bradford B Krahe, Ralf

PloS one, 2011-09, Vol.6 (9), p.e23161 [Periódico revisado por pares]

United States: Public Library of Science

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8
Accelerating Medicines Partnership: Parkinson's Disease. Genetic Resource
Accelerating Medicines Partnership: Parkinson's Disease. Genetic Resource
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Accelerating Medicines Partnership: Parkinson's Disease. Genetic Resource

Iwaki, Hirotaka ; Leonard, Hampton L. ; Makarious, Mary B. ; Bookman, Matt ; Landin, Barry ; Vismer, David ; Casey, Bradford ; Gibbs, J. Raphael ; Hernandez, Dena G. ; Blauwendraat, Cornelis ; Vitale, Daniel ; Song, Yeajin ; Kumar, Dinesh ; Dalgard, Clifton L. ; Sadeghi, Mahdiar ; Dong, Xianjun ; Misquitta, Leonie ; Scholz, Sonja W. ; Scherzer, Clemens R. ; Nalls, Mike A. ; Biswas, Shameek ; Singleton, Andrew B.

Movement disorders, 2021-08, Vol.36 (8), p.1795-1804 [Periódico revisado por pares]

Hoboken, USA: John Wiley & Sons, Inc

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9
Genome-wide association study reveals genetic risk underlying Parkinson's disease
Genome-wide association study reveals genetic risk underlying Parkinson's disease
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Genome-wide association study reveals genetic risk underlying Parkinson's disease

Singleton, Andrew B ; Gasser, Thomas ; Simón-Sánchez, Javier ; Schulte, Claudia ; Bras, Jose M ; Sharma, Manu ; Gibbs, J Raphael ; Berg, Daniela ; Paisan-Ruiz, Coro ; Lichtner, Peter ; Scholz, Sonja W ; Hernandez, Dena G ; Krüger, Rejko ; Federoff, Monica ; Klein, Christine ; Goate, Alison ; Perlmutter, Joel ; Bonin, Michael ; Nalls, Michael A ; Illig, Thomas ; Gieger, Christian ; Houlden, Henry ; Steffens, Michael ; Okun, Michael S ; Racette, Brad A ; Cookson, Mark R ; Foote, Kelly D ; Fernandez, Hubert H ; Traynor, Bryan J ; Schreiber, Stefan ; Arepalli, Sampath ; Zonozi, Ryan ; Gwinn, Katrina ; van der Brug, Marcel ; Lopez, Grisel ; Chanock, Stephen J ; Schatzkin, Arthur ; Park, Yikyung ; Hollenbeck, Albert ; Gao, Jianjun ; Huang, Xuemei ; Wood, Nick W ; Lorenz, Delia ; Deuschl, Günther ; Chen, Honglei ; Riess, Olaf ; Hardy, John A

Nature genetics, 2009-12, Vol.41 (12), p.1308-1312 [Periódico revisado por pares]

New York, NY: Nature Publishing Group

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10
Baseline genetic associations in the Parkinson's Progression Markers Initiative (PPMI)
Baseline genetic associations in the Parkinson's Progression Markers Initiative (PPMI)
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Baseline genetic associations in the Parkinson's Progression Markers Initiative (PPMI)

Nalls, Mike A. ; Keller, Margaux F. ; Hernandez, Dena G. ; Chen, Lan ; Stone, David J. ; Singleton, Andrew B.

Movement disorders, 2016-01, Vol.31 (1), p.79-85 [Periódico revisado por pares]

United States: Blackwell Publishing Ltd

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